VAERS 2021 Database www.vaers.hhs.gov

Main Page | All 2021 Deaths | Videos
VAERS Updated: 11/12/2021
** VAERS DATABASE Last updated: November 12, 2021**
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Manufacturers

Total Manufacturer
199,106MODERNA
36,710JANSSEN
5,381PFIZER\BIONTECH
2,555GLAXOSMITHKLINE BIOLOGICALS
1,469UNKNOWN MANUFACTURER
897MERCK & CO. INC.
627SEQIRUS, INC.
112DYNAVAX TECHNOLOGIES CORPORATION
91SANOFI PASTEUR
75NOVARTIS VACCINES AND DIAGNOSTICS
40EMERGENT BIOSOLUTIONS
14PAXVAX
12TEVA PHARMACEUTICALS
12PROTEIN SCIENCES CORPORATION
9PFIZER\WYETH
4BERNA BIOTECH, LTD.
4SMITHKLINE BEECHAM
3INTERCELL AG
1MEDIMMUNE VACCINES, INC.
1CSL LIMITED

COVID19 Lot Number

VAX LOT Total
2S9CL7,949
7,473
2,547
1,506
1,187
1,051
1,049
s0294561,043
866
IMM209861
816
UT7065MA766
657
579
U62828AA563
557
538
U6737AA516
515
S034636506
4F472471
458
P100253275449
444
276563436
429
418
4BH32414
MENVEO404
PP9L5362
UJ446AA337
319
306
290
271
49TM3270
R1B252M253
4F472179
933622147
C5763AA144
CW3116134
3Y7NL126
UNK114
113
ARBA141A105
104
103
96
300057A90
79
1F4EB73
R1B743M62
56
UJ090AA55
51
UH894AB46
45
UNK44
UNK42
42
EJ168638
Unknown36
35
34
32
32
26
el128424
24
A115A22
22
EN620222
21
UNK20
20
19
Z127A19
19
17
JEV18K95E15
12
111798PI12
10
A739088
No batch number8
3333324181078
6
6
TAR356
5
5
U6935AA5
UNK5
4
unknown4
3
2
55RB72
2
2
2
2
2
U7124AA2
JEV18A68E2
2
ABYB05BA1
1
1
1
1
AMVA436A1
1
1
TJ3521
A130A; VIS give1
1
U7140BB1
1
1
SP UP016AA1
1
1808P08802/ESV01
037K20A300,947
EL1284288,578
57,766
1,432

Incidents per State

State Total
82,750
CA62,821
FL38,209
TX36,512
NY34,921
PA23,646
IN23,622
IL20,597
MI19,590
OH19,426
NJ18,413
NC16,769
GA15,932
WA15,351
VA15,234
MA14,876
AZ14,206
MN12,940
MD12,656
CO11,908
WI11,425
MO10,240
TN9,685
OR8,768
KY8,437
CT8,300
SC6,700
OK6,293
AL5,692
LA5,025
IA4,825
KS4,821
UT4,637
NV4,374
NM3,967
AR3,807
ME3,161
NH3,096
NE2,918
MS2,859
ID2,785
WV2,469
HI2,459
PR2,417
MT2,414
RI2,076
DE1,868
AK1,830
VT1,734
DC1,715
ND1,388
SD1,269
WY866
GU118
VI69
AS47
MP29
MH8
XB6
FM4
QM3
XV2
XL1

ID: 1692688
Sex: F
Age:
State: FL

Vax Date: 04/10/2021
Onset Date:
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: A filling pop in her mouth; Headache; Nausea; This is a spontaneous report from a contactable consumer or other non hcp (Patient) from a Pfizer sponsored program COVAX Support. A 39-years-old female patient received second dose of bnt162b2 (BNT162B2, PFIZER-BIOTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 10Apr2021 as single dose for covid-19 immunisation. Medical history included has some allergy issues and is experiencing a runny nose and post nasal drip and an irritated sore throat, She is unsure if its allergies or a cold from an unknown date and unknown if ongoing. Historical vaccine included first dose of BNT162B2 for covid-19 immunization. The patient concomitant medications were not reported. It was reported that patient set to receive her first dose of the Pfizer vaccine today but has some allergy issues and is experiencing a runny nose and post nasal drip and an irritated sore throat. She is unsure if its allergies or a cold. Can she still receive the vaccine today and wanted to know it be efficacious. She is not currently taking any medications for her allergy symptoms. Upon date 12Apr2021 it was reported that patient received second dose and experienced a filling pop in her mouth and has a dentist appointment tomorrow morning. Asked if it is okay to have the appointment or in case they will give medication like Novocaine after receiving the second dose. Upon date 13Apr2021 it was reported that She has an upcoming dental appointment, and may need some fillings. She wants to know if it is safe to have the dental procedure done. Also reported she has been experiencing a headache that has been coming and going and some nausea. Neither symptom lasts long. She was asking if this could be because of the second dose, and how long the symptoms could last. The outcome for the events was reported as unknown at the time of this report. No follow-up attempts are possible; information about lot/batch number cannot been obtained

Other Meds:

Current Illness:

ID: 1692689
Sex: F
Age:
State:

Vax Date: 02/25/2021
Onset Date:
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025L20A
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: Soreness; feeling stiff; This is a spontaneous report from a contactable consumer, based on information received by Pfizer (manufacturer control number: EC-2021-089449), for BNT162B2. A female patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; solution for injection, Lot Number: Unknown), via unspecified route of administration, on unspecified date as a dose number unknown, single for COVID-19 immunization. The patient medical history included C55 uterine cancer, Shingles (she has been on Gabapentin since her Shingles outbreak). The patient started taking other medication on 25Feb2021 which included lenvatinib mesylate (LENVIMA) and pembrolizumab (KEYTRUDA). On an unspecified date the patient advised that she had been feeling stiff and sore the last few days. Patient got the COVID shot from Pfizer a few days ago. Soreness appeared after that. Patient advised some of the discomfort follows the same areas as she shingles outbreak, she had last year. Patient had been on gabapentin since her Shingles outbreak. Patient receive the treatment of tylenol and occasional a tramadol for soreness and stiffness. Patient was advised to seek healthcare care professional guidance on what to do for this issue. Patient believed that it was a combination of lenvima, keytruda, and the COVID shot that are causing patient's issues. The outcome of the events was unknown. Follow-up attempts completed. No further information expected.

Other Meds: LENVIMA; KEYTRUDA

Current Illness:

ID: 1692690
Sex: F
Age:
State: NH

Vax Date: 01/25/2021
Onset Date:
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: EL1284
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Chest discomfort, Dysphagia, Pain in extremity, Visual impairment

Symptoms: Sore arm; This is a spontaneous report from a contactable consumer (Patient). A 23-year-old non-pregnant female patient received of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Lot number: EL3247) via unspecified route of administration, in left arm on 25Jan2021 12:00 PM as a dose 1, single for COVID-19 immunization. The patient medical history included amoxicillin allergy. The concomitant medication of the patient was not reported. Patient had not received any other vaccine within four weeks prior to the COVID vaccine and patient had not received any other medications in two weeks vaccination. The patient had not COVID prior to vaccination and not tested post COVID vaccination. On unspecified date patient experienced sore arm only after administration of first dose of BNT162B2. Outcome of event was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1692691
Sex: F
Age:
State: ME

Vax Date: 03/05/2021
Onset Date: 03/01/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: unknown
Dose Series: UNK
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: She was shaking all over; she was trying to throw up; She felt pretty bad; This is a spontaneous report received from a contactable consumer (patient husband). A 86-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EN6204, NDC number: unknown, Expiry date: 30Jun2021), via an unspecified route of administration on 05Mar2021 (age at vaccination was 86 years) as dose 1, single for COVID-19 immunisation. Medical history and concomitant medications were not reported. The reporter says he and his wife had the first shot 5 Mar, Friday and today he thought he was going to lose her. He wondered if patient had a reaction or something to the vaccine. On an unspecified date in Mar2021, the patient was shaking all over and patient was trying to throw up, felt pretty bad. The reporter was trying to see if that was a reaction to the vaccine. Primary care reported as the reporter called them and they said someone would get a hold of them but they are having the same problem, there are so many calls ahead and they are going to know the same thing, she was shaking all over. The reporter just wanted to make sure everything was on the up and up. The patient slept most of the afternoon and got up and was feeling better now. The reporter says they are looking for the phone number to the doctor's office. They are still looking for the number. The reporter says we can continue, and they will keep looking for it. No investigation assessment reported. Outcome of the events was resolved on an unspecified date in 2021. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1692692
Sex: F
Age:
State: PA

Vax Date: 02/17/2021
Onset Date: 02/18/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site pruritus, Injection site swelling, Injection site warmth

Symptoms: sore arm; This is a spontaneous report from a contactable consumer. This case is for 1st dose. A 65-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EL9266) via an unspecified route of administration, administered in Arm Left on 17Feb2021 16:30 (at the age of 65-year-old) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included cerebrovascular accident, blood cholesterol, blood pressure abnormal, pain. Concomitant medication(s) included warfarin (WARFARIN) 5mg; take once daily orally taken for Stroke from Oct2020 and ongoing; rosuvastatin calcium (ROSUVASTATIN CALCIUM) 40mg; take once daily orally taken for cholesterol from an unspecified start date and ongoing; amlodipine besilate (AMLODIPINE BESILATE) 2.5mg take once daily orally taken for Blood pressure from Jan2021 and ongoing; paracetamol (TYLENOL) 500mg; take as needed taken for pain from an unspecified start date and ongoing. The patient experienced sore arm on 18Feb2021. Prior Vaccinations (within 4 weeks) reported as no. Patient did not any AE(s) require a visit to emergency room and physician office. The outcome of event was recovered after 20 days on 10Mar2021. No follow-up attempts are possible. No further information is expected.

Other Meds: WARFARIN; ROSUVASTATIN CALCIUM; AMLODIPINE BESILATE; TYLENOL

Current Illness:

ID: 1692693
Sex: F
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 09/11/2021
Hospital:

Vax Type: FLUC4
Manufacturer: SEQIRUS, INC.
Vax Name: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT)
Lot: 276563
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Chills, Confusional state, Eye inflammation, Headache, Laboratory test

Symptoms: body ache; chills; headache; This is a spontaneous report received from a contactable consumer (patient) from a Pfizer sponsored program. A female patient of unspecified age received BNT162B2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, batch/lot number: not reported, expiration date: not reported) via an unspecified route of administration on an unknown date as DOSE NUMBER UNKNOWN, SINGLE for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. It was reported that patient had mild reaction, chills, body ache and headache she wanted to know if she could take Dayquil/Nightquil. Outcome of the events was unknown. Follow-up attempts are completed. No further information was expected.

Other Meds:

Current Illness:

ID: 1692694
Sex: F
Age:
State: NY

Vax Date:
Onset Date:
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: pain in arm; This is a spontaneous report from a Pfizer Sponsored Program. A contactable female patient reported that, a female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 1 via an unspecified route of administration, administered on an unspecified date (Batch/Lot number was not reported) as DOSE 1, SINGLE for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient wanted to know if she could take pain medication after receiving the first covid vaccine due to pain in arm and wanting to take pain medicine. Outcome of the event was unknown. Information on the lot/batch number has been requested. Follow-up (11May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1692695
Sex: U
Age:
State:

Vax Date: 03/10/2021
Onset Date: 03/01/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: soreness in arm; This is a spontaneous report from a contactable consumer or other non-HCP (measurable supplier, patient). A patient of unspecified age and gender received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number- UNKNOWN) via an unspecified route of administration on 10Mar2021 as dose 1, single for COVID-19 immunization. Patient medical history and concomitant medications were not reported. The patient experienced soreness in arm on an unspecified date in Mar2021. Event took place after use of product. The outcome of the event was unknown. Follow up letter has been generated for further information. Follow-up (12May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1692696
Sex: F
Age:
State: CA

Vax Date: 03/01/2021
Onset Date: 03/01/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: lower back pain; This is a spontaneous report received from a contactable consumer via Pfizer sponsored program COVAX US Support. A female patient (reporter's mother) of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported) by an unspecified route of administration on 01Mar2021 as DOSE 1, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced lower back pain on an unspecified date on Mar2021 and the reporter wants to know more about the side effects. The outcome of the event unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1692697
Sex: F
Age:
State: NJ

Vax Date: 03/09/2021
Onset Date: 03/09/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J201A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: 1st dose of Covid 19 Vaccine (03/09/21) within a minute after the Vaccine she felt light headed and very tired, that feeling continued and felt very tired and then that same day; 1st dose of Covid 19 Vaccine (03/09/21) within a minute after the Vaccine she felt light headed and very tired, that feeling continued and felt very tired and then that same day; This is a spontaneous report from a Pfizer-sponsored program received from a contactable consumer, the patient. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number was not reported), dose 1 via an unspecified route of administration on 09Mar2021 as dose 1, single for covid-19 immunization. The patient medical history and concomitant medications were not reported. Patient had 1st dose of covid 19 vaccine and within a minute after the vaccine she felt lightheaded and very tired, that feeling continued and felt very tired and then that same day, she woke up again and with the same feeling. The outcome of the event was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1692698
Sex: U
Age:
State: WI

Vax Date: 03/04/2021
Onset Date: 03/01/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data: Test Name: Fasting blood sugar; Result Unstructured Data: Test Result:average of 98; Test Date: 20210311; Test Name: Fasting blood sugar; Result Unstructured Data: Test Result:97; Comments: Back to normal; Test Date: 202103; Test Name: Fasting blood sugar; Result Unstructured Data: Test Result:average of 113.6

Allergies:

Symptom List: Vaccination site erythema, Vaccination site pruritus, Vaccination site swelling

Symptoms: The first 5 days of patient's fasting blood sugar rose from an average of 98 to an average of 113.6; This is a spontaneous report from a contactable consumer (Patient). A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection) via an unspecified route of administration on 04Mar2021 (Batch/Lot number was not reported) as dose number unknown, single for COVID-19 immunisation. Medical history included pre-diabetic and take blood sugar twice a day and record it in a spreadsheet. The patient concomitant medications were not reported. The patient stated that he/she received Covid-19 vaccine on 04Mar2021, and it appeared to have worked great. No issues of concern Just 1 piece of feedback. The patient stated that he/she was pre-diabetic and took blood sugar twice a day and record it in an spreadsheet. The first 5 days of patient's fasting blood sugar rose from an average of 98 to an average of 113.6. It was back to normal the morning (11Mar2021) when the patient reported was 97. No complaint just some feedback. The patient reported that he/she felt great. Outcome of the event was recovered on 11Mar2021. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1692699
Sex: F
Age:
State: FL

Vax Date: 03/06/2021
Onset Date:
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039k20a
Dose Series: 1
Vax Route: SYR
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: Pain in her arm; Soreness in her breast; pain in her nipple; Lymph node; This is spontaneous report received from a contactable consumer reported for her daughter. A 37-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number: unknown, Expiration date: unknown) via an unspecified route of administration, administered at an unspecified anatomical location on 06Mar2021 (age at vaccination was 37 years) as dose 1, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient had the first Pfizer COVID vaccine on 06Mar2021 and immediately came home with pain in her arm on the side where she got the shot, pain in her nipple on the side that she got the shot and soreness in her breast on the same side as vaccine administration on an unspecified date, but the symptoms resolved. She stated that it went away after couple of days. She took some Tylenol and was fine. She stated that she knew there were lymph nodes in the area, but wanted to know if that was normal and how to treat it. She wanted to know if possible if it could be a lymph node. She wanted to see if there were other cases where not the lymph node but in the actual breast itself. She received the response which stated that lymphadenopathy is a commonly reported AE from the clinical trials but does not specify location of the lymph nodes in question. No information for timing of onset or duration. The patients in the trial were allowed to treat symptoms with acetaminophen or NSAIDs, if medically appropriate. The caller was referred back to HCP for evaluation and treatment. The outcome of the events pain in her arm, soreness in her breast and pain in her nipple was resolved on an unspecified date in 2021. The outcome of the event lymph node was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1692700
Sex: F
Age:
State: MI

Vax Date: 03/01/2021
Onset Date:
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Blood pressure decreased, Chest pain, Chills, Confusional state, Decreased appetite

Symptoms: sinus infection; This is a spontaneous report from a Pfizer Sponsored Program Covax support via a contactable consumer (patient, self-reported). A Female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date were not reported), via an unspecified route of administration, on 01Mar2021, as a single dose for COVID-19 immunization. The patient's medical history included cancer and osteopetrosis (Prolia shots to prevent osteopetrosis). Concomitant medications were not reported. On an unspecified date, the patient experienced sinus infection. The patient was scheduled to start Prolia shots to pre-vent osteopetrosis and wanted to know if able to get injections prior to her second dose of the vaccine scheduled for 22Mar2021. She had to delay first injection of Prolia due to sinus infection after March 1st. Outcome of the event was unknown. Information on the lot/batch number has been requested. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1692701
Sex: F
Age:
State: CA

Vax Date: 03/08/2021
Onset Date: 03/10/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20-2A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Dyspnoea, Fatigue, Feeling abnormal, Head discomfort, Headache

Symptoms: feeling pain in the right side of the arm; feeling pain in the right side of the arm and neck that goes from shoulder to the top of her ear; Extreme headache/Blood rushing straight to the top of her head like it was going to explode; crying; could not move her right arm and shoulder/hard time turning her neck; felt like her right shoulder was dislocated; All of a sudden she stated experiencing this feeling and pain, unknown if it is a pinched nerve or muscle; All of a sudden she stated experiencing this feeling and pain, unknown if it is a pinched nerve or muscle; I've ever experienced!! I thought I was about to die or have a brain aneurysm; The initial safety information received was reporting only non-serious adverse drug reactions, Upon receipt of follow-up information on [31Aug2021], this case now contains serious adverse reactions. Information processed together. This is a spontaneous report from a contactable consumer (patient). A 39-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in Arm Left on 08Mar2021 16:00 at 39-years-old (Batch/Lot Number: EL9264) as dose 1, single for COVID-19 immunization. Medical history included Sensory Neuropathy from Dec2019 and ongoing (Diagnosed while hospitalized for this in Dec2019), ongoing Anxiety, Asthma from 1995 and ongoing (around age of 13 years). Vaccination Facility Type: health clinic. Concomitant medications included lorazepam taken for Anxiety from Jun2015 and ongoing (Most recently restarted around time of COVID-19 pandemic which really exacerbated anxiety so doctor put her back on Lorazepam as needed); gabapentin taken for Sensory neuropathy from 22Dec2020 and ongoing; cyanocobalamin (VITAMIN B12) taken for Deficiency from Dec2019 and ongoing; vitamin d taken for Deficiency from Dec2019 and ongoing. Caller mentions that she got the first dose of the Pfizer covid 19 vaccine this past Monday March 8th on her left arm and then on Thursday she started feeling pain in the right side of the arm and neck that goes from shoulder to the top of her ear. Also she experienced extreme headache like exploding in the top of her skull like an orgasm and also was the same intensity on Friday. She was not sure if the headache was caused by the vaccine or was spontaneous. She wanted to know whether she continued to get the second dose of the vaccine. Caller mentions that she is concerned about the low representability of her race in the clinical trial and that her side effects would be disregarded because of that. She thinks that the amount of people like her, of the trial is not representative of the whole population living in the country and the side effects that are taking in the trial are not disclosed for the races that were participating on it. She reported experiencing side effects that that she is not sure are connected to the vaccine, but that she believes are connected to the vaccine. She reported it is like you know how sometimes you don't know if it is 100% related to something or not, but she has never really experienced these side effects like this before the Pfizer-BioNTech COVID-19 Vaccine. Side effects reported include, pain which started evening of 11Mar2021. She woke in the middle of the night, probably into Friday, 12Mar2021 at that point, and had really, extremely bad pain in her right arm and was crying; she could not move her right arm and shoulder; felt like her right shoulder was dislocated. She has never had a dislocated shoulder but she felt like maybe it would feel like that event because she could not move her right arm and shoulder. She went back to sleep that night. By the time she woke up later on 12Mar2021 the pain was gone and she was able to rotate her shoulder and arm, able to perform regular movement, range of motion; events kind of went away for a while. When she woke up Saturday morning, 13Mar2021, all of a sudden she started experiencing this feeling and pain, unknown if it is a pinched nerve or muscle, but that feeling from like her lower right shoulder all the way up to behind the top of her right ear and has a hard time turning her neck. She is taking Tylenol and Ibuprofen for pain and inflammation. She reported another side effect that is pretty personal, and she does not know if it is connected to the vaccine, but she feels like it is connected to the vaccine because she has never experienced this until after she was administered the Pfizer-BioNTech COVID-19 Vaccine: On Thursday, 11Mar2021 she had the most extreme headache from orgasming. She did not know if it was an isolated event so she said let her try it again the next day and it happened again on Friday, 12Mar2021, it was so painful, she was like oh my God, she could feel the blood rushing straight to the top of her head like it was going to explode. The event on Thursday, 11Mar2021 was worse than the event on Friday, 12Mar2021 12Mar2021 event was almost as bad as on Thursday, 11Mar2021 but she stopped midway because she thought if she finished her head might explode. The extreme headache from orgasming had an interesting lingering effect, it did not go away right away; the initial rush of pain that went to the very top of her head took a while to subside on Thursday, 11Mar2021, did not go away probably until unknown time-she took some pain killers because the pain was just that bad and she fell asleep. When she woke up on Friday, 12Mar2021 the pain was there so she took 1 Tylenol that evening. Side effects outcome, She thought this would go away, but it has not gone away she cannot say side effects have worsened but they have not improved, remained pretty much persistent. Pain level on scale of 1-10 she reported as 8 at this time. She did plan to get the second dose as scheduled for 29Mar2021 but she does have second thoughts based on the side effects she is experiencing but will that prevent her from getting the second dose more than likely not. She just has her concerns about these side effects which hopefully are not permanent. It was further reported that the patient received the 1st dose in her left shoulder on 08Mar2021, on 10Mar2021 she woke up in the middle of the night crying because her right shoulder felt like it was dislocated. She could not move her right arm. When she woke up about 9 am. She had a sharp painful pinched nerve, running from the top of the back of my right ear, all the way down to her shoulder wing blade. Then when orgasming. She felt all the blood in her body rushing to the top of her head/skull. The most painful headache she had ever experienced!! She thought she was about to die or have a brain aneurysm! 2nd attempt on 11Mar2021- happened again! She called them, then her doctor. The patient experienced feeling pain in the right side of the arm on 11Mar2021 with outcome of not recovered, feeling pain in the right side of the arm and neck that goes from shoulder to the top of her ear on 10Mar2021 with outcome of not recovered, extreme headache/blood rushing straight to the top of her head like it was going to explode on 10Mar2021 with outcome of not recovered, crying on 10Mar2021 with outcome of not recovered, could not move her right arm and shoulder/hard time turning her neck on 10Mar2021 with outcome of not recovered, felt like her right shoulder was dislocated on 10Mar2021 with outcome of not recovered, all of a sudden she stated experiencing this feeling and pain, unknown if it is a pinched nerve or muscle, but that feeling from like her lower right shoulder all the way up to behind the top of her right ear and has a hard time turning her neck on 10Mar2021 with outcome of not recovered, brain aneurysm on 10Mar2021 with outcome of unknown. Therapeutic measures were taken as a result of events except brain aneurysm. The patient was advised not to take second dose. Seriousness criteria was reported as serous, Important medical event. No follow-up attempts are needed. No further information is expected.

Other Meds: LORAZEPAM; GABAPENTIN; VITAMIN B12 [CYANOCOBALAMIN]; VITAMIN D

Current Illness: Anxiety (COVID-19 pandemic really exacerbated anxiety.); Asthma (around age of 13 years); Sensory neuropathy (Diagnosed while hospitalized for this in Dec2019.)

ID: 1692702
Sex: M
Age:
State: MI

Vax Date:
Onset Date:
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Heart rate decreased, Heart rate increased, Hypertension, Injection site pain, Musculoskeletal chest pain

Symptoms: sinus infection; This is a spontaneous report received from contactable consumer (patient) via Pfizer sponsored program. A male patient of unspecified age received first dose of BNT162B2 (Pfizer covid-19 vaccine, Solution for injection, Lot Number were not reported) via on an unspecified route on unknown date as DOSE 1, SINGLE for COVID-19 Immunization. On an unspecified date patient had experienced sinus infection. And reported that had first dose already second dose due to get on 16th wanted to know if he can get second dose or should he postpone it. Therapeutic measures were taken for the event sinus infection and included treatment with Zpack. The clinical outcome of the event was unknown. Information on the lot/batch number has been requested. Follow-up (11May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1692703
Sex: F
Age:
State: NM

Vax Date: 01/29/2021
Onset Date: 01/29/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Nausea, Pain, Pain in extremity, Paraesthesia oral, Pyrexia

Symptoms: upper midsternal chest pressure; skin with redness to upper chest and neck; worsened with swallowing; This is a spontaneous report from a contactable other healthcare professional. A 19-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EL3246), intramuscular on 29Jan2021 14:35 (at the age of 19-years-old) as dose 1, single for covid-19 immunisation. It was unknown if the patient was pregnant at the time of vaccination. The vaccine was administered at the public health department. The patient medical history included childhood asthma. The patient does have a history of anaphylaxis with all fish. Concomitant medications included melatonin; and diphenhydramine hydrochloride (BENADRYL) both were taken for an unspecified indication, start and stop date were not reported; epinephrine (EPIPEN); and medroxyprogesterone acetate (DEPOPROVERA) both were taken for anaphylactic reaction, start and stop date were not reported. The patient previously took prednisone, and experienced anaphylaxis. The patient received 1st dose of vaccine approximately at 14:35. At 15:00 approximately 25 minutes post vaccination patient started feeling upper midsternal chest pressure, worsened with swallowing. Patient's skin with redness to upper chest and neck. The patient received liquid oral Benadryl 50 mg. The outcome of the events was recovered. No follow-up attempts are possible; information about lot/batch number already obtained.

Other Meds: MELATONIN; BENADRYL; EPIPEN; DEPOPROVERA

Current Illness:

ID: 1692704
Sex: F
Age:
State: CA

Vax Date: 03/11/2021
Onset Date: 03/15/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: DTAPHEPBIP
Manufacturer: GLAXOSMITHKLINE BIOLOGICALS
Vax Name: DTAP + HEPB + IPV (PEDIARIX)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data:

Allergies:

Symptom List: SARS-CoV-2 antibody test, SARS-CoV-2 test negative

Symptoms: Allergic reaction to my right eye; This is a spontaneous report from a contactable consumer (patient).A 34-years-old non-pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 11Mar2021 at 08:00 (Batch/Lot number was not reported, Expiry date not reported) (at the age of 34-years-old) as dose 2, single for COVID-19 immunization. The patient did not had any medical history and no allergies to medications, food, or other products. Concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19, Since the vaccination, the patient has not been tested for COVID-19. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 18Feb2021 at 09:15 (Batch/Lot number was not reported, Expiry date not reported) as dose 1, single for COVID-19 immunization. On 15Mar2021 at 20:00, the patient experienced allergic reaction to right eye. It was reported that Same thing happened to her sister who got the shot at the same time. No treatment received for the adverse event. The patient had not yet recovered from the event. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021289428 same reporter/drug/AE with different patient

Other Meds:

Current Illness:

ID: 1692705
Sex: F
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 09/11/2021
Hospital:

Vax Type: HIBV
Manufacturer: MERCK & CO. INC.
Vax Name: HIB (PEDVAXHIB)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data: Test Date: 20210205; Test Name: Lab test; Result Unstructured Data: Test Result:Unknown results; Comments: "Yes, it's a long result but yes, the date was 05Feb"

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: I was just aching with the first injection; This is a spontaneous report from a contactable consumer (patient). An 85-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot Number and Expiration date was not reported), via an unspecified route of administration on an unspecified date as DOSE 1, SINGLE for covid-19 immunisation. Medical history included high blood pressure from an unknown date and unknown if ongoing. Concomitant medication stated as yes, details were not provided (other products: yes). The patient experienced just aching with the first injection on an unspecified date with outcome of unknown. The patient underwent lab tests and procedures which included laboratory test: unknown results on 05Feb2021 and stated it was a long result. Patient called after she got the first injection because she had so many questions that weren't answered for her (not clarified if called in Pfizer drug safety, hence case was marked as initial). Height was stated as probably about 5'3". Facility name where the vaccine was administered, consumer stated as continuing care residency, well they were issued by or distributed by (pharmacy name) pharmacy. When asked about concomitant medication, patient stated she take lot of medications, and to hold, to let her get list of meds. Patient stated she had no problem; she was just aching with the first injection. When asked about product details (LOT# and expiration date) for first dose: Consumer stated to have the first date and guessed as 18Jan and said no. Consumer was informed about Pfizer Medical information department. Patient wanted to know was the injection effective even though she had that itching, concern because she has long list of symptoms that Pfizer gave her, the literature that she had and that was not one of them and just wanted to be sure because it was different, and her results of receiving and having a medication effectiveness was not hampered. Clinical outcome of event was unknown. Information on lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1692706
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/11/2021
Hospital:

Vax Type: PNC13
Manufacturer: PFIZER\WYETH
Vax Name: PNEUMO (PREVNAR13)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: Headache; head is killing me, it is stressing me out; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot Number: EN6202; Expiration date was not reported), via an unspecified route of administration on an unspecified date as DOSE NUMBER UNKNOWN, SINGLE for covid-19 immunisation. Medical history included traumatic Brain Injury, seasonal allergies from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. The patient experienced headache on an unspecified date. Therapeutic measures were taken as a result of headache. Patient had the Covid shot the day before this report (19Mar2021) and got a headache that couldn't get rid of. Patient asked what to do to get rid of the headache (manufacturer not clarified, hence is this a Pfizer product tab left unchecked). Stated to get a bit of a headache then and it does not go away. Consumer was informed about Pfizer Medical Information department. Consumer further stated to transfer as quick as you can do it because patient head was killing patient, it was stressing patient out. Patient stated that between the allergies and the TBI and this Covid shot got a terrible headache patient couldn't get rid of it. And headache was causing patient a lot of stress right then. Consumer stated, got a TBI that was number 1. Got Traumatic Brain Injury (Intent: History) and number 2 was that patient take medications for allergy (Further not clarified over the call hence captured as unspecified medication). So, between the allergies and the TBI and this Covid shot patient got a terrible headache patient couldn't get rid of it. Patient took Tylenol the day before this report. Consumer informed about Pfizer Medical Information Department and about the role of Pfizer Drug safety. When asked about LOT#: Consumer stated, "I can't understand you it's hard to me to understand you because of you accent I am not trying to be rude I just don't understand when you, the second was EN6204." (unclear, so retained as EN6202). Consumer stated that he/she was going to take Ibuprofen or Advil, the headache was killing. Product details (NDC# UPC# and Treatment) and Pharmacy details could not be probed as consumer was unwilling to share further information. Hence further probing could not be done. Limited information available over the call. Clinical outcome of events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1692707
Sex: F
Age:
State:

Vax Date: 03/04/2021
Onset Date:
Rec V Date: 09/11/2021
Hospital:

Vax Type: RV1
Manufacturer: GLAXOSMITHKLINE BIOLOGICALS
Vax Name: ROTAVIRUS (ROTARIX)
Lot:
Dose Series: 1
Vax Route: PO
Vax Site: MO

Lab Data:

Allergies:

Symptom List: Blood pressure increased, Chest discomfort, Heart rate increased

Symptoms: in the past I have gotten a lump in my neck, like a swollen gland that eventually goes away; This is a spontaneous report from a contactable consumer (patient). A 59-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), via an unspecified route of administration on 04Mar2021 (Batch/Lot number was not reported) as dose 1, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient previously received flu vaccine on an unspecified date. Caller received first dose 04Mar2021 and second dose scheduled for 25Mar2021. Caller asked if she should get second injection on the same arm and stated: in the past she had gotten a lump in her neck, like a swollen gland that eventually went away. Her Doctor told her to definitely go get the Covid19 vaccination, the lump usually resolves. Caller mentioned they do not know if the lump was caused with another vaccine or with the flu vaccine in the past. The outcome of event was recovered on an unspecified date. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1692708
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: Eh9899
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site pruritus, Injection site swelling, Lymph node pain, Lymphadenopathy

Symptoms: runny nose; This is a spontaneous report from a contactable other hcp. A 58-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot Number and Expiry date was not reported), via an unspecified route of administration on unspecified date as dose 2, single for COVID-19 immunization. The Patient Medical history included, surgeries in January from an unknown date and unknown if ongoing. The patient concomitant medications was not reported. The patient previously took xeljanz xr in the past and it stopped working. Previously patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: solution for injection, Batch/Lot Number and Expiry date was not reported), via an unspecified route of administration on unspecified date as dose 1, single for COVID-19 immunization. The Patient has been off treatment as she had surgeries in January and had both COVID-19 vaccines while off Xeljanz. On Unspecified date, the patient experienced runny nose. She is having anxiety because her son is being deployed in a month. The outcome for the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1692709
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: strong pain in the vaccinated site six hours after the vaccination; This is a spontaneous report from a non-contactable consumer. An adult patient of an unspecified gender received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection), via an unspecified route of administration on an unspecified date (reported as 610, CCYYMM) (Batch/Lot number was not reported) as dose 1, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced strong pain in the vaccinated site six hours after the vaccination with the outcome of unknown. The patient also received the second dose of BNT162B2 on an unspecified date in Jan2021 (Batch/Lot number was not reported) for COVID-19 immunisation. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1692710
Sex: M
Age:
State: IN

Vax Date: 03/22/2021
Onset Date:
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Name: Pain; Result Unstructured Data: Test Result:at 8 or 9

Allergies:

Symptom List: Chills, Dizziness, Injection site pain, Myalgia, Pyrexia

Symptoms: Feeling strange/felt his body changing/"a strange feeling" throughout his whole body; Fever all over body; I thought I would just lay down in bed and I could not do that; got 3 or 4 hours of sleep in chair; Pain in every joint in body, toes, ankles, knees everywhere; Pain in every joint in body, toes, ankles, knees everywhere; Looked at my hand, took out the thumb and it was like firm; Lied down on the bed and immediately, it was like I was drugged, just gone; felt body was just floating down into the bed; developed an "intense pain" all over his body/the pain he experienced after the doses of vaccine, he would rate as an 8 or 9; slept for 10-10.5 hours; This is a spontaneous report from a contactable consumer (patient himself). A 78-years-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number: EW0158; Expiration date: unknown) via an unspecified route of administration on 13Apr2021 (at age of 78-years-old) as DOSE 2, SINGLE and patient had received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number: ER2513; Expiration date: unknown) via an unspecified route of administration, administered in Arm Left on 22Mar2021 16:10 (at age of 78-years-old) as DOSE 1, SINGLE for COVID-19 immunization. Medical history included ongoing arthritis; diagnosed 20 years ago and COVID-19 from 29Nov2020 to an unknown date. There were no concomitant medications reported. Family medical history relevant to AE(s) was none. AE(s) following prior vaccinations was none. On an unspecified date it was reported that, the consumer stated, he had the Pfizer COVID-19 Vaccine shot (later confirmed) yesterday in left arm and it was like nothing. He hardly felt the shot. He sat for 15 minutes and they had served and felt fine, so he left. When he got in the car, drove home and he was fine for probably about 4 hours, it was actually like 5 hours. But then around 10:30 when he normally get to bed, he went into bed and thought feel really strange here. And had heart problems in the past but did not think this was heart problem at all. But anyway, thought just sit in the chair and he had a fever all over body, it was not painful at all, no pain whatsoever. But just felt something was going to happen. So thought he would just lay down in bed and he could not do that, so he sat in the chair and got 3 or 4 hours of sleep. And woke up at 4 o' clock in the morning exactly and the pain was at 8 or 9. Every joint, and he do have arthritis but can walk around, can be all fine. He was 78, but the pain in every joint in body, toes, ankles, knees everywhere. In fact, it was interesting, when he sat here in the chair it did pain, he looked at hand and took out the thumb and it was like firm. And whenever he put it in front of hand, the pain would be incredible from that joint and every finger hurt but it was pretty much awful but he didn't know. He thought he should go the Emergency room in the Hospital and he was like, he was just going to stay here for a little while. So, he sat there for like another hour and he thought well maybe if he will try, he can go back to sleep. He went and lied down on the bed and immediately, it was like he was drugged, just gone and felt his body was just floating down into the bed and he went to really, really comfortable sleep for 2 hours. He had set the alarm for 2 hours later. 2 hours later, when the alarm went off, he put his feet out of the edge of bed and did stand up, he was dramatically better. His joints were bad but they were not bad as before. Consumer further stated, he had the virus on 29Nov2020. He went to the emergency room at the hospital and they shot this liquid in my arm and took an hour and they took an hour for observation. They had injected in his arm and they said since you had this, you were not going to be able to get virus for three or four months. Consumer stated, he did not need to talk to anybody else. Just turned that information over to the people, that might be helpful to them so that they know that this could happen to somebody. The pain was very, very bad, every joint. When he got out of bed, he could barely walk, it was that bad and thought what was going on here. But now, every hour that goes by, he get better and better to the point that hopefully, that will pass. So, he just wanted to let you know, maybe he can help somebody else. States when he had his second shot, he was told since he had the infusion and waited 3 months, he thought this time he wouldn't go through the pain. Caller stated it was every bit as bad as the first for 16 hours the most intense part. Stated he had pain from one tip of his shoulder to other and into base of the skull and every joint in his body hurt like hell. States someone brought him some Tylenol and it definitely made the pain easier. States he wanted to call and let Pfizer know and he was afraid if he takes the vaccine again in a year that he will get that intense pain. States he is absolutely amazed at how bad it could be. Caller stated he does feel it is a combination of the vaccine and his arthritis. States somehow the way it attacked his joints, he felt pain in all his joints, toes, ankles but he doesn't have arthritis in those, just his knees and hands little finger, nothing like all the rest of the joints. States with the second vaccine her could tell that going to have an issue. States in the period of 5- 10 minutes, he had the same situation that he had before but this time he didn't have the 45minute preamble of saying was he having a heart attack? he was very calm and had a strange feeling in his body and then it went away that he had with the first vaccine. After the first dose, he felt his body changing and reported "a strange feeling" throughout his whole body that lasted for about an hour. Then he developed an intense pain all over his body that lasted for 16 hours, he slept for 10-10.5 hours, and woke up with pain that lasted a few more hours then resolved. The same thing happened after the second dose, but without the strange feeling. He said he was used to a dull pain from his arthritis, that he would rate as 0.5 out of 10; but the pain he experienced after the doses of vaccine, he would rate as an 8 or 9. But wanted to know if other people have reported symptoms or an experience like his or not. Adverse event did not require a visit to emergency room physician office. Therapeutic measures were taken as a result of developed an intense pain all over his body/the pain he experienced after the doses of vaccine, he would rate as an 8 or 9 (pain). The patient underwent lab tests and procedures which included pain assessment: at 8 or 9 on an unspecified date. The outcome of all events was recovering.

Other Meds:

Current Illness: Arthritis (Arthritis Diagnosed 20 years ago.)

ID: 1692711
Sex: F
Age:
State: OH

Vax Date: 03/18/2021
Onset Date: 03/18/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011L20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: it feels like it is effecting the nerves.; She is a little nervous; my tongue started feeling tingly and the right corner of my mouth felt numb/have a little numbness/feels weird; my tongue started feeling tingly and the right corner of my mouth felt numb/have a little numbness/feels weird; Thursday, she could feel something moving up the right cheek; she had twitching under her eye and it looked swollen on the right side compared to left side; she had twitching under her eye and it looked swollen on the right side compared to left side; then on Thursday 3/25 felt movement from the right corner of my mouth up the right cheek, Friday evening (3/26) had twitching under my right eye and the right side of my face was a little swollen; Still have a little numbness, still get twitching on & off & face is still a little swollen on the right side; Headache; nausea; dizziness/woozy; stomach pain; very tired/fatigued; This is a spontaneous report from a contactable consumer or other non hcp. A 53-years-old non-pregnant female patient received bnt162b2 first dose (BNT162B2, Solution for injection, Batch/Lot Number: EN6206) via an unspecified route of administration in Arm Left on 18Mar2021 12:45 (age at vaccination: 54 Years) as DOSE 1, SINGLE for covid-19 immunisation (at pharmacy).Patient was not pregnant at the time of vaccination. Patient didn't received other vaccines within 4 weeks prior to vaccination, patient received other medications within 2weeks of vaccination. Medical history included headache from an unknown date and unknown if ongoing , impaired gastric emptying from an unknown date and unknown if ongoing , fatigue from an unknown date and unknown if ongoing , gastroesophageal reflux disease from an unknown date and unknown if ongoing , fibromyalgia from an unknown date and unknown if ongoing , hypertension from an unknown date and unknown if ongoing , thyroiditis from an unknown date and unknown if ongoing , drug hypersensitivity from an unknown date and unknown if ongoing Allergies to medications, food, or other products: Sulfa, Tegatrol, hypersensitivity from an unknown date and unknown if ongoing Allergies to medications, food, or other products: Sulfa, Tegatrol. The patient's concomitant medications were not reported. Patient was not diagnosed with covid-19 prior to vaccination, patient was not tested with covid-19 to post vaccination. The patient experienced headache on 18Mar2021 14:30, nausea on 18Mar2021 14:30, dizziness/woozy on 18Mar2021 14:30 with outcome of recovering , stomach pain on 18Mar2021 14:30, very tired/fatigued on 18Mar2021 14:30, my tongue started feeling tingly and the right corner of my mouth felt numb/have a little numbness/feels weird on 20Mar2021 14:30, my tongue started feeling tingly and the right corner of my mouth felt numb/have a little numbness/feels weird on 20Mar2021 14:30, then on Thursday 3/25 felt movement from the right corner of my mouth up the right cheek, Friday evening (3/26) had twitching under my right eye and the right side of my face was a little swollen on 18Mar2021 14:30, still have a little numbness, still get twitching on & off & face is still a little swollen on the right side on 18Mar2021 14:30, Thursday, she could feel something moving up the right cheek on 20Mar2021, she had twitching under her eye and it looked swollen on the right side compared to left side on 20Mar2021, she had twitching under her eye and it looked swollen on the right side compared to left side on 20Mar2021 with outcome of unknown , it feels like it is effecting the nerves. on an unspecified date, she is a little nervous on an unspecified date. No therapeutic measures were taken with events. The outcome of the events headache, nausea, dizziness, abdominal pain upper, fatigue, paraesthesia oral, hypoaesthesia oral was recovering, the outcome of the events dyskinesia, blepharospasm, eye swelling, nerve injury, nervousness was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1692712
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: she noted of "every" joint & body was aching & after receiving first dose covid 19 vaccine (pfizer); she feels achy; This is a spontaneous report from a Pfizer- sponsored program. A contactable other healthcare professional and a contactable consumer (patient) reported that a 47-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number not reported), via an unspecified route of administration on an unspecified date as single dose for covid-19 immunisation; tofacitinib citrate (XELJANZ XR), oral from 21Jan2021 and ongoing, at 11 mg, 1x/day for rheumatoid arthritis. Medical history included thinning of nail, recurring bad acne, rheumatoid arthritis, and depressed. Concomitant medication included benzoyl peroxide (MANUFACTURER UNKNOWN) for acne and methotrexate (MANUFACTURER). The patient reported that after exercising for a few days on an unspecified date, she noted of "every" joint & body was aching & after receiving first dose covid 19 vaccine (Pfizer), she feels "achy" (unknown if this is muscle/joint), resolved after two days. MD was aware. The action taken in response to the events for tofacitinib citrate was unknown. The patient recovered from the events on an unspecified date. No follow up attempts are needed. Further information of lot/batch number not obtained.

Other Meds: BENZOYL PEROXIDE; METHOTREXATE

Current Illness:

ID: 1692713
Sex: U
Age:
State:

Vax Date: 02/08/2021
Onset Date: 02/10/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data: Test Date: 20210210; Test Name: blood test; Result Unstructured Data: Test Result:stage-3 chronic kidney disease; Test Name: ultrasound; Result Unstructured Data: Test Result:nothing wrong with kidney, not even a tiny little; Comments: nothing wrong with kidney, not even a tiny little cyst

Allergies:

Symptom List: Arthralgia, Chills, Headache, Mobility decreased, Myalgia

Symptoms: stage-3 chronic kidney disease; This is a spontaneous report from a contactable consumer, the patient. A patient of unspecified age and gender received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: UKNOWN) via unspecified route on 08Feb2021 as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot number: UNKNOWN) on 15Jan2021 as a single dose for COVID-19 immunization. Two days after the second dose (10Feb2021), the patient went in for routine blood test that he/she has taken every year. Patient never had a problem with kidneys before, it had always been normal, but 2 days after that vaccine, the patient had abnormal reading on kidney that put him/her in a stage-3 chronic kidney disease (10Feb2021). Then doctor sent the patient for an ultrasound (unspecified date). There was nothing wrong with kidney, not even a tiny little cyst. Patient inquired if the vaccine can possibly interfere with blood test specially kidney function. The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1692714
Sex: F
Age:
State: IL

Vax Date: 04/03/2021
Onset Date: 04/06/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: Cycle started on cycle day 25 . It's been extremely heavy extremely hard cramps; Cycle started on cycle day 25 . It's been extremely heavy extremely hard cramps; spotting; This is a spontaneous report from a contactable consumer (patient). A 37-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: ER8733), dose 2 via an unspecified route of administration, administered in Arm Left on 03Apr2021 15:45 (at the age of 37-year-old) as dose 2, single for COVID-19 immunization. The patient medical history was not reported. Concomitant medication(s) included ascorbic acid, betacarotene, biotin, calcium carbonate, calcium pantothenate, chromium, colecalciferol, copper, cyanocobalamin, ferrous fumarate, folic acid, magnesium oxide, manganese, nicotinamide, potassium iodide, pyridoxine hydrochloride, riboflavin, selenium, thiamine hydrochloride, tocopheryl acetate, zinc (PRENATAL [ASCORBIC ACID;BETACAROTENE;BIOTIN;CALCIUM CARBONATE;CALCIUM PANTOTHENATE;CHROMIUM;COLECALCIFEROL;COPPER;CYANOCOBALAMIN;FERROUS FUMARATE;FOLIC ACID;MAGNESIUM OXIDE;MANGANESE;NICOTINAMIDE;POTASSIUM IODIDE;PYRIDOXINE HYDROCHLORIDE;RIBOFLAVIN;S) taken for an unspecified indication, start and stop date were not reported (Other medications in two weeks). Patient pregnant was unknown and pregnant at the time of vaccination was unknown. The patient previously received first dose of BNT162B2 (Lot number: EN6204) via an unspecified route of administration, administered in Arm Left on 13Mar2021 06:45 PM (at the age of 37-year-old) for COVID-19 immunization. Facility type vaccine was other. The patient did not receive any other vaccine in four weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Post vaccination, the patient had not been tested for COVID-19. Patient had no known allergies. Reported that started spotting on cycle day 23. Cycle started on cycle day 25. It's been extremely heavy extremely hard cramps (06Apr2021 06:00). I was always on time. Never early or late. My cycles were like click work at 28 days. There was no treatment for the events. The clinical outcome of events was unknown. Follow-up attempts completed. No further information expected.

Other Meds: PRENATAL [ASCORBIC ACID;BETACAROTENE;BIOTIN;CALCIUM CARBONATE;CALCIUM PANTOTHENATE;CHROMIUM;COLECALC

Current Illness:

ID: 1692715
Sex: F
Age:
State:

Vax Date: 04/13/2021
Onset Date: 04/13/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: injection site has mild soreness; a weird taste in my mouth; constricted my throat/a tightness in the back of my throat, as though the glands were swollen; a tightness in the back of my throat, as though the glands were swollen; constricted my throat making it uncomfortable to swallow; discomfort; felt weakness in my whole body; walking felt strange; This is a spontaneous report from a non-contactable consumer (patient) reported herself that a 41-years-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, batch/ lot number: EN6207), via an unknown route of administration in left arm on 13Apr2021 at 09:45 as single dose (at age of 41-years old) for COVID-19 immunization. The patient's medical history included diabetes mellitus from an unknown date to unknown if ongoing. No known allergies. Concomitant medications were not reported. No other vaccine in four weeks. Other medication in two weeks was multi-vitamins. On 13Apr2021 at 09:45, the patient experienced injection site has mild soreness even 24 hours later. Shortly after injection, during the initial 15 minutes waiting period until 5 or 6 hours later, there was a weird taste in her mouth and a tightness in the back of her throat, as though the glands were swollen and constricted her throat making it uncomfortable to swallow. There was no pain. Between a rating of 1 to 10, the discomfort level was about 5. She also felt weakness in her whole body and walking felt strange and lasted for the entire day. No COVID prior vaccination. No COVID tested post vaccination. No treatment received for events. The outcome of the events was recovered on an unspecified date in Apr2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1692716
Sex: F
Age:
State: NJ

Vax Date: 04/12/2021
Onset Date: 04/12/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data: Test Date: 20210412; Test Name: Blood pressure; Result Unstructured Data: Test Result:went up

Allergies:

Symptom List: Headache, Heart rate increased, Injection site erythema, Injection site pain, Injection site swelling

Symptoms: Difficulty breathingRapid heart palpitationsTight chest and throat Blood pressure went up; Difficulty breathingRapid heart palpitationsTight chest and throat Blood pressure went up; Difficulty breathingRapid heart palpitationsTight chest and throat Blood pressure went up; Difficulty breathingRapid heart palpitationsTight chest and throat Blood pressure went up; Difficulty breathingRapid heart palpitationsTight chest and throat Blood pressure went up; This is a spontaneous report from a contactable consumer (patient) reported herself that a 39-years-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection), dose 1 via an unspecified route of administration, administered in Arm Left on 12Apr2021 15:15 (Batch/Lot Number: ER8729) as dose 1, single (at the age of 39-years-old) for covid-19 immunization. Facility type vaccine was other. The patient's medical history included Sjorgens Syndrome. She was allergic to pineapple and Penicillin. Concomitant medications were not reported. No other vaccine in four weeks. On 12Apr2021 at 17:00, the patient experienced difficulty breathing, rapid heart palpitations, tight chest and throat, and blood pressure went up. Events resulted in doctor or other healthcare professional office or clinic visit. No COVID prior vaccination. No COVID tested post vaccination. No treatment received. The outcome of the events was resolved on an unspecified date in Apr2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1692717
Sex: F
Age:
State:

Vax Date: 04/01/2021
Onset Date: 04/01/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: I am still feeling a little warm off and on.; I am getting some muscle pain in my lower legs, like a tightness.; Some muscle issues on the side of her calf area, like the inside of her leg area is hurting; I am getting some muscle pain in my lower legs, like a tightness.; I am getting some muscle pain in my lower legs, like a tightness.; This is a spontaneous report received from a contactable consumer (patient) reported for herself that a female patient of an unknown age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, batch/lot number: unknown, expiry date: not provided), via an unknown route of administration on 01Apr2021 as single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unknown date in Apr2021, the patient experienced "I am still feeling a little warm off and on", while she had her shot like two weeks ago. She was not running a fever or anything. She was getting some muscle pain in her lower legs, like a tightness. Some muscle issues on the side of her calf area, like the inside of her leg area was hurting. She gets a little hot too but that was the only two things she has experienced. She wanted to be sure that this was a normal thing. No, this report was not related to a study or programme. The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1692718
Sex: F
Age:
State: UT

Vax Date: 04/12/2021
Onset Date: 04/15/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site pain

Symptoms: Menstruation started 3 weeks early, much heavier than normal; Menstruation started 3 weeks early, much heavier than normal; This is a spontaneous report from a contactable consumer (patient). A 24-year-old non pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EWO162) via an unspecified route of administration, administered in Arm Left on 12Apr2021 15:00 (at the age of 24 years old) as dose 1, single for COVID-19 immunisation. Medical history included food allergy (Known allergies- Food allergies). No known medication allergies, no allergies to anything in COVID vaccine. The patient's concomitant medications were not reported. Patient did not received other vaccine within four weeks of COVID vaccine. Patient did not have COVID prior to vaccination. The patient experienced menstruation started 3 weeks early, much heavier than normal on 15Apr2021. No treatment were given for the adverse event. Patient did not tested for COVID post vaccination. Outcome of all the events were not resolved. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1692719
Sex: M
Age:
State: ID

Vax Date: 04/06/2021
Onset Date: 04/06/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site induration, Injection site pruritus, Injection site swelling, Injection site warmth

Symptoms: Soreness in arm for 10 days; Heaviness and shortness and breathing; Cough; This is a spontaneous report from a contactable consumer (patient). A elderly male (Age:68; Unit: Unknown) patient received bnt162b2 (BNT162B2, Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 06Apr2021 12:00 as DOSE NUMBER UNKNOWN, SINGLE for covid-19 immunisation. Medical history included covid-19 from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. Prior to vaccination the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. On 06Apr2021 03:00 the patient experienced soreness in arm for 10 day, heaviness and shortness and breathing, cough. Outcome of Event was Not recovered. No follow-up attempts are possible. Information about Lot/Batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1692720
Sex: F
Age:
State: TX

Vax Date: 04/11/2021
Onset Date: 04/11/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011j20a
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data: Test Name: heart rate; Result Unstructured Data: Test Result:unknown results

Allergies:

Symptom List: Chills, Dizziness, Nausea, Pain, Tachycardia

Symptoms: my throat starting getting tight and was dry; my throat starting getting tight and was dry; This is a spontaneous report from a contactable consumer (patient). A 69-year-old non pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: solution for injection, lot number: EP7533, expiration date was not reported), via an unspecified route of administration, administered in right arm on 11Apr2021 13:15 (at the age of 69-years-old) as dose 2, single for covid-19 immunization. The patient medical history was not reported. Concomitant medications included omeprazole (20 mg), escitalopram (10 mg), simvastatin (40 mg). Other medications patient received in two weeks included omeprazole 20mg, escitalopram 10 mg, simvastatin 40mg. The patient historical vaccine included first dose of BNT162B2 (Lot number: EN6207, expiration date was not reported), via an unspecified route of administration, administered in right arm on 14Mar2021 01:00pm (at the age of 69-years-old) as dose 1, single for covid-19 immunization. Patient did not receive other vaccine in four weeks. The patient does not have any allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. It was reported that on 11Apr2021 01:15 PM, on second shot - Within 10 minutes her throat starting getting tight and was dry. EMS checked her heart rate and listened to her heart. She waited an additional 30 minutes before they had her leave. Symptoms stayed for about 3 hours and went away. The patient underwent lab tests and procedures which included heart rate: unknown results on an unspecified date. No treatment was received for the adverse event. The outcome of the events was recovered on an unspecified date of 2021. No follow-up attempts are possible. No further information is expected.

Other Meds: OMEPRAZOLE; ESCITALOPRAM; SIMVASTATIN

Current Illness:

ID: 1692721
Sex: F
Age:
State: KS

Vax Date: 04/01/2021
Onset Date: 04/01/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Name: blood pressure; Result Unstructured Data: Test Result:164/86; Comments: blood pressure at 164/86; Test Name: Heart rate; Result Unstructured Data: Test Result:79 bpm; Comments: Heart rate decreased to 79 bpm; Test Date: 202104; Test Name: Heart rate; Result Unstructured Data: Test Result:90+bpm; Test Name: Pulse; Result Unstructured Data: Test Result:Pulse after discharge 88

Allergies:

Symptom List: Tremor

Symptoms: raised heart rate to 90+bpm; GI Nausea; shortness of breath; Rash on legs/ Rash on both arms and torso; Itching; loose bowel movement; Fatigue; red finger tips/bright red palms; red nail area; purple fingers to knuckle area; This is a spontaneous report from a contactable consumer (Patient). A 63-years-old non pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EP7533), dose 1 via an unspecified route of administration, administered in Arm Left in Apr2021 at 02:30 PM (Age at vaccination: 63 years) as dose 1, single for covid-19 immunisation. Patient had known allergies to penicillin, sulfa, ibuprofen, flu vaccine, chocolate, pepper, citrus, chemical senitiviies. Other medical history included asthma, IBS, allergies. Concomitant medications included vitamin d [vitamin d nos] (VITAMIN D [VITAMIN D NOS]). Patient did not receive other vaccines in 4 weeks. The patient experienced raised heart rate to 90+bpm, gi nausea, shortness of breath, rash on legs/ rash on both arms and torso, itching, loose bowel movement, fatigue, red fingertips/bright red palms, red nail area, purple fingers to knuckle area in Apr2021. Immediately after injection raised heart rate to 90+bpm, GI Nausea. Within 5 minutes shortness of breath occured. 50mg of Benadryl (Diphenhydra-mine HCL) within 10 minutes of vaccine was given. Heart rate decreased to 79 bpm; shortness of breath was decreased within 25 minutes of first Benadryl dose. Rash on legs first 30 mins. Heart monitored at ER for two hours with no incident found. Pulse after discharge was 88 and blood pressure was at 164/86. There was Rash on both arms and torso later in the day along with itching. Aggressive rash/itching continued on arms for 4 for days requiring Benadryl 50mg/4 hours. Day 5 Benadryl reduced to 50mg/6 hour then 8 hours and by day 6 rash was gone. Shortness of breath subsided within 2 hours. Nausea resulted in 1 loose bowel movement within first hour post vaccine with no other GI issues. Fatigue was on day 2 only. Covid fingers day 3 thru day 5, with stronger symptoms on left hand. Symptoms changed but included red fingertips, red nail area, purple fingers to knuckle area, bright red palms. Treatment for the events included Benadryl 50mg/4 hour for 4.5 days. Patient did not have COVID prior vaccination. Patient did not test COVID post vaccination. The patient underwent lab tests and procedures which included blood pressure measurement: 164/86 on blood pressure at 164/86, raised heart rate to 90+bpm in Apr2021, heart rate: 79 bpm, Heart rate decreased to 79 bpm, heart rate: pulse after discharge was 88. The outcome of the events was recovered in 2021. No follow-up attempts are possible. No further information is expected.

Other Meds: VITAMIN D [VITAMIN D NOS]

Current Illness:

ID: 1692722
Sex: F
Age:
State: IN

Vax Date: 04/06/2021
Onset Date: 04/11/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: Off label use; Drug use in unapproved population; clogged milk ducts; This is a spontaneous report from a contactable consumer or other non hcp (Patient). A 36-years-old female patient (non-pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: ER8732), dose 1 via an unspecified route of administration, administered in Arm Right on 06Apr2021 17:00 (at the age of 36 years old) as dose 1, single for covid-19 immunisation. Medical history included from an unknown date and unknown if ongoing. No known allergies. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient concomitant medication was not reported. The patient didn't received other medications within 2 weeks of vaccination. Patient stated I am a breast feeding mom. 5 days after receiving the vaccine I began experiencing clogged milk ducts on 06Apr2021 17:00. No treatment was received in response to the adverse events. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, patient was not tested for COVID-19. At the time of reporting, the outcome of the events were recovering.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021427749 baby case

Other Meds:

Current Illness:

ID: 1692723
Sex: F
Age:
State: MO

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: UNK
Manufacturer: UNKNOWN MANUFACTURER
Vax Name: VACCINE NOT SPECIFIED (NO BRAND NAME)
Lot:
Dose Series: UNK
Vax Route: SYR
Vax Site: UN

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site induration, Injection site pruritus, Injection site swelling, Myalgia

Symptoms: Muscle and joint pain in upper left arm; Muscle and joint pain in upper left arm; unable to raise left arm as high as my right arm since second vaccine; numbness in left arm while lying on my left side; extreme fatigue; frequent headaches; This is a spontaneous report from a contactable nurse (patient) reported herself that a 36-years-old non-pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, batch/ lot number: unknown), via an unknown route of administration in left arm on 11Jan2021 at 13:15 (at the age of 36-years-old) as single for COVID-19 immunization at hospital. The patient's medical history included ADHD (Attention deficit hyperactivity disorder) and depression; both were from an unknown date to unknown if ongoing. She had no known allergies. Concomitant medications included duloxetine hydrochloride (CYMBALTA) and lisdexamfetamine mesylate (VYVANSE); both were taken for an unknown indication from an unknown date. No other vaccine in four weeks. The patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, batch/ lot number: unknown), via an unknown route of administration in left arm on 16Dec2020 at 13:00 (at the age of 36-years-old) as single for COVID-19 immunization. On 11Jan2021 at 20:00, the patient experienced muscle and joint pain in upper left arm, unable to raise left arm as high as my right arm since second vaccine, numbness in left arm while lying on my left side, extreme fatigue and frequent headaches. The events resulted in doctor or other healthcare professional office/clinic visit. No COVID prior vaccination. No COVID tested post vaccination. No treatment received. The outcome of the events was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: CYMBALTA; VYVANSE

Current Illness:

ID: 1692724
Sex: F
Age:
State: GA

Vax Date: 04/17/2021
Onset Date: 04/18/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Cough, Limb discomfort, Pain, SARS-CoV-2 test positive

Symptoms: Chills with chattering teeth.; Tightness in throat; difficulty breathing; lightheadedness; This is a spontaneous report from a contactable consumer. This consumer (patient) reported that, a 50-years-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection), dose 2 via an unspecified route of administration, administered in Arm Left on 17Apr2021 09:00 (Batch/Lot Number: Ew0162) as dose 2, single (at age of 50-years old) for covid-19 immunization. The patient medical history included allergies to Histamines, FQ drugs, and cigarette smoke from an unknown date and unknown if ongoing. Concomitant medication included vitamin c (ASCORBIC ACID) taken for an unspecified indication, start and stop date were not reported. The patient previously took first dose of bnt162b2 Solution for injection, via an unspecified route of administration, administered in Arm Left on 27Mar 2021 09:00 AM (Batch/Lot Number: En6207) as single dose (at age of 50-years old) for covid-19 immunization. There was no other vaccine in four weeks. No covid prior vaccination and no covid tested post vaccination. The patient experienced chills with chattering teeth, tightness in throat, difficulty breathing, lightheadedness on 18Apr2021. It was reported that, 15 hrs after injection, Chills with chattering teeth and Tightness in throat that would come and go. Lasted 4 hours. Some difficulty breathing (Took Benedryl) Some lightheadedness on 18Apr2021. The patient taken Benedryl for difficulty breathing and no treatment for other events. The outcome of the events was resolving at the time of reporting. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021343956 similar report from same reporter

Other Meds: VITAMIN C [ASCORBIC ACID]

Current Illness:

ID: 1692725
Sex: M
Age:
State: NY

Vax Date: 04/12/2021
Onset Date: 04/01/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: flu symptoms; son has been sick; having pain in his back and up to his neck; itching/itching where the shot was injected; muscle aches; chills; Lot of mucus coming up; arm was red; brain fog; swollen lymph nodes under arm; Lump on arm where he got injection; did not feel well; This is a spontaneous report from a contactable consumer (mother) reported for her son. This report 1 of 3 (consumer and her son's father both had side effects). A 17-years-old male patient received first dose of BNT162B2 (Pfizer-Biontech COVID-19 Vaccine, Solution for injection, batch/lot number and expiry date: not reported), via an unknown route of administration in right arm on 12Apr2021 (at the age of 17-years-old) as dose 1 single for COVID-19 immunisation at drug store, it was like 10:45 am. The patient's medical history and family medical history relevant to events were none. Concomitant medication was not reported. History of all previous immunization with the Pfizer vaccine considered as suspect was none. All vaccines administered on same date with the Pfizer vaccine considered as suspect was none. Any other vaccinations within four weeks prior to the first administration date of the suspect vaccine was none. On an unknown date in Apr2021, the patient experienced swollen lymph nodes under arm, lump on arm where he got injection, did not feel well. On 14Apr2021, arm was red duration of event was one day, brain fog, muscle aches, chills duration of event was one day, lot of mucus coming up. On 15Apr2021, itching/itching where the shot was injected. The patient has swollen lymph nodes under his arm (caller noticed that within the second day after getting the vaccine and was getting better); a big lump where the injection was, arm was red (there were lumps are on his arm and look like he was flexing. He was itching and it was red yesterday but no longer red. There was a lump there. He was getting better, it was scary. He noticed that the second day, but now he was experiencing brain fog.); itching (just at the shot site, around there. It was his right arm. This morning was when it happened, it was still going on), brain fog (he forgot what he was doing at work. He was cooking and was like what was I doing. He noticed this yesterday. That has gotten better) and muscle aches (he said this happened when he first got the shot after they left the drug store. He said within an hour he started having pain in his back and up to his neck. He said he went to bed and it went away. Then, he called and said he did not feel well. Caller told her son to come home, and he came home). Caller stated these were kind of like flu symptoms and that was normal. He has chills (happened within an hour after the vaccine, within a half hour after injection. Caller's son said he was good now), itching where the shot was injected and lot of mucus coming up (caller adds that her son was spitting up a lot of mucus. This did not start until he got the shot. It was still going on). Caller got the shot and was sick for two hours, and then was fine but her son has been sick since Monday. Caller called the doctor yesterday and was told that the reactions are normal. No additional information. He did not take anything as treatment, because he did not want to. Caller told him to maybe take something, and she adds maybe he took Tylenol but she does not know. The doctor said that if he did not get better, to make an appointment, but she thinks he was getting better. The outcome of the events swollen lymph nodes under arm, lump on arm where he got injection, brain fog was recovering. The outcome of the events arm was red and chills was recovered on 15Apr2021. The outcome of the events lot of mucus coming up and itching/itching where the shot was injected was not recovered, while the outcome of the remaining events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1692726
Sex: M
Age:
State: MO

Vax Date: 04/07/2021
Onset Date: 04/07/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data: Test Name: Blood pressure; Result Unstructured Data: Test Result:between 115/70 and 128/74; Comments: I usually sit between 115/70 and 128/74; Test Date: 20210407; Test Name: Blood pressure; Result Unstructured Data: Test Result:elevated (between 150 and 160 as the upper number); Comments: between 150 and 160 as the upper number with a heart beat of 110 bpm; Test Name: Heart beat; Result Unstructured Data: Test Result:68 bpm; Test Date: 20210407; Test Name: Heart beat; Result Unstructured Data: Test Result:110 bpm; Test Date: 20210407; Test Name: oxygen; Result Unstructured Data: Test Result:normal

Allergies:

Symptom List: Injection site erythema, Injection site pain, Injection site swelling

Symptoms: tightness in my face; slight lightheadedness; something akin to a hotflash; heart beat became unnervingly very rapid; elevated blood pressure (between 150 and 160 as the upper number with a heart beat of 110 bpm; This is a spontaneous report from a contactable consumer (patient) reported himself. A 37-years-old male patient received first dose of BNT162B2 (Pfizer-Biontech COVID-19 Vaccine, Solution for injection, batch/lot number: EW0151), via an unspecified route of administration in left arm on 07Apr2021 at 11:00 (at the age of 37-years-old) as dose 1, single for COVID-19 immunisation. Facility type vaccine reported as other. The patient's medical history was reported as none. No known allergies. The patient concomitant medications were not reported. The patient did not receive any other vaccine in four weeks. The patient was not diagnosed with Covid-19, prior vaccination. The patient was not tested positive for covid-19, post vaccination. On 07Apr2021 at 11:00, the patient experienced within the first 5 minutes after receiving the shot, I began having tightness in my face, slight lightheadedness, something akin to a hotflash, and my heart beat became unnervingly very rapid. I went with an EMT to get checkout. I was told I had elevated blood pressure (between 150 and 160 as the upper number with a heart beat of 110 bpm- I usually sit between 115/70 and 128/74 and around 68 bpm). I was told my blood oxygen looked normal by the EMT. After about 1-2 hours after the shot, I was fine. My blood pressure and heartbeat returned to my normal levels. The patient did not received treatment for the events. The outcome of the events was recovered on an unspecified date. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1692727
Sex: U
Age:
State: NY

Vax Date:
Onset Date:
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: EK9231
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Chills, Feeling cold, Feeling hot, Myalgia, Pain

Symptoms: Shingles; This is a spontaneous report from a contactable consumer or other non hcp. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection, Lot number and expiration date was not reported), via an unspecified route of administration on an unspecified date as dose number unknown, single for COVID-19 immunization. The patient's concomitant medications and medical history were not reported. The patient experienced shingles on an unspecified date. The outcome of the event was unknown. No follow-up attempts are needed. Information about Lot/Batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC same reporter/AE/drug, different patient

Other Meds:

Current Illness:

ID: 1692728
Sex: F
Age:
State: TN

Vax Date: 04/11/2021
Onset Date: 04/11/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Date: 20210411; Test Name: BP; Result Unstructured Data: Test Result:80/52; Comments: Her blood pressure had bottomed out to 80/52; Test Date: 20210411; Test Name: BP; Result Unstructured Data: Test Result:80/52; Comments: I continued checking her bp that came up to 82/50; Test Date: 20210411; Test Name: BP; Result Unstructured Data: Test Result:100/60; Comments: another recheck of 100/60

Allergies:

Symptom List: Pain in extremity

Symptoms: malaise; tired/fatigue; everything was "turning black"; blood pressure had bottomed out to 80/52; slumped over; This is a spontaneous report from a contactable Nurse (patient mother). A 17-years-old non pregnant female patient received first dose of BNT162B2(PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection) via an unspecified route of administration, administered in Arm Right on 11Apr2021 13:15 (Batch/Lot number was not reported) (at the age of 17-year-old) for COVID-19 immunisation. The patient had no other medical history. Patient had no covid prior vaccination. Patient did not receive any other vaccines within 4weeks. Concomitant medications included sulfamethoxazole, trimethoprim (BACTRIM) taken for an unspecified indication, start and stop date were not reported. The patient previously took clindamycin and experienced allergy. On 11Apr2021 13:30 the patient experienced malaise, tired, everything was "turning black", blood pressure had bottomed out to 80/52, fatigued, slumped over. Approximately 5-10 minutes post vaccination, patient began to appear malaise. She complained that she felt extremely tired. Next, she stated that everything was "turning black". The pharmacist who gave the vaccine was no where to be found. Patient mother ran and got the NP at the clinic w/in the pharmacy to check her BP. NP stated to mother that she could not hear a BP. Patient mother asked if she could use her stethoscope to hear a BP, as patient mother a RN. Her blood pressure had bottomed out to 80/52. We got her feet up quickly as she was beginning to look very fatigued and slumped over. Patient mother continued to check her blood pressure after the NP left daughter and patient mother in the waiting area to go and continue to see her other clinic pts. Patient mother called 911 to get her daughter some medical assistance as patient mother was starting to panic. Patient mother continued checking her bp that came up to 82/50 and another recheck of 100/60. The EMT arrived maybe 5 min or so later. She continued to have the normal fatigue x2 days. AE resulted in Doctor or other healthcare professional office/clinic visit. AE treatment included called EMT to vaccine site, hydrated, feet elevated to recover blood pressure back to normal limits. The patient did not tested covid post vaccination. Outcome of the events was recovered in 2021. Information about lot/batch number has been requested.

Other Meds: BACTRIM

Current Illness:

ID: 1692729
Sex: F
Age:
State: NY

Vax Date: 01/05/2021
Onset Date: 01/20/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 2
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Abnormal behaviour, Adverse reaction, Anger, Asthma

Symptoms: Wasn't feeling well; Shingles; This is a spontaneous report from a contactable consumer. This 39 year-old non-pregnant female consumer (Patient) reported that she received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: EL0142) via an unspecified route of administration on 05Jan2021 at 04;30 PM (at 39-year-old) in left arm as dose 1, single for COVID-19 immunization. The patient had no medical history and no allergies. The patient received Healther birth control pills in two weeks. It was mentioned that no other vaccine was received in four weeks, the patient did not have Covid prior vaccination and was not tested for covid post vaccination. Two weeks after the first dose on 20Jan2021 at 01:00 pm patient was not feeling well and went to (withheld) Urgent Care and was diagnosed with Shingles. She had never had Shingles and also did not have any underlying illnesses. The event resulted in emergency room visit. She was treated with Valtrex for events. On an unknown date in 2021 the patient recovered. No follow-up attempts were possible. No further information was expected.

Other Meds:

Current Illness:

ID: 1692730
Sex: M
Age:
State: NY

Vax Date: 04/16/2021
Onset Date: 04/17/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Consciousness fluctuating, Crying, Dry skin, Epistaxis, Headache

Symptoms: Shingles developed on back and arms day after second Pfizer covid vaccine.; This is a spontaneous report from a contactable consumer. A 40-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection. Batch/Lot Number: EP7533), dose 2 via an unspecified route of administration, administered in right arm on 16Apr2021 at 10:00 (at the age of 40-years-old) as DOSE 2, SINGLE for COVID-19 immunization. Medical history included type 1 diabetes mellitus and testis cancer (malignant neoplasm of testis 20 years ago) from an unknown date and unknown if ongoing. Drug hypersensitivity (Known allergies: amoxicillin; penicillin) from an unknown date and unknown if ongoing. Historical vaccine included: first dose of BNT162B2 (COMIRANTY; Solution for injection; Batch/Lot Number: EN6204) as dose 1, single administered in left arm on Mar2021 at 11:00AM (at the age of 40-years-old) for COVID-19 immunization. Concomitant medications included losartan (LOSARTAN), rosuvastatin (ROSUVASTATIN), apixaban (ELIQUIS) and insulin lispro (HUMALOG) taken for an unspecified indication, start and stop date were not reported other medications received in two weeks. COVID prior vaccination: Unknown. No other vaccine in four weeks. Facility type vaccine at pharmacy or drug store. On 17Apr2021 at 06:00, the patient experienced shingles developed on back and arms day after second. Adverse events resulted in Doctor or other health care professional office/clinic visit, Emergency room/department or urgent care. Adverse event treatment include anti-viral medication and pain medication. No COVID tested post vaccination. The outcome of the event was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: LOSARTAN; ROSUVASTATIN; ELIQUIS; HUMALOG

Current Illness:

ID: 1692731
Sex: F
Age:
State: FL

Vax Date: 03/20/2021
Onset Date: 03/23/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Hypotonia, Lethargy, Respiratory rate decreased, Screaming, Skin warm

Symptoms: Shingles; This is a spontaneous report received from a contactable consumer or other non-health care professional (patient). A 47-years-old non-pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EN6955), via an unspecified route of administration, administered in Arm Left on 20Mar2021 17:45 (at the age of 47-years-old) as dose 1, single for COVID-19 immunisation. Medical history included chickenpox virus from an unknown date and unknown if ongoing. Concomitant medications included levothyroxine sodium (LEVOTHYROXINE SODIUM), fluticasone propionate, salmeterol xinafoate (ADVAIR), fluticasone (FLUTICASONE) taken for an unspecified indication, start and stop date were not reported. The patient previously took Symbicort and experienced hypersensitivity. The patient experienced shingles on 23Mar2021. Patient received treatment Medication for the chickenpox virus, pain and gel. Patient visited Emergency room/department or urgent care. The outcome of the events was reported as recovering. No follow-up attempts are needed, information about lot/batch number cannot be obtained.

Other Meds: LEVOTHYROXINE SODIUM; ADVAIR; FLUTICASONE

Current Illness:

ID: 1692732
Sex: M
Age:
State: NY

Vax Date: 03/09/2021
Onset Date: 03/25/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 026LZOA
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: Shingles; This is a spontaneous report from a contactable consumer (patient himself). A 46-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) via unspecified route of administration, in left arm on 09Mar2021 09:45 (age at vaccination: 46-years-old) as dose 2, single for covid-19 immunisation. Historical vaccine included first dose of BNT162B2 (Lot number: EL3247), via unspecified route of administration, in left arm on 17Feb2021 09:45 AM as dose 1, single for covid-19 immunisation. Facility type vaccine was workplace clinic. Medical history of patient was not reported. No other vaccine in four weeks was administered to the patient. Concomitant medication included Acutane 10mg, taken for unspecified indication, start and stop date unknown. Patient had no known allergies. On 25Mar2021 15:00, patient experienced shingles. The event resulted in doctor or other healthcare professional office/clinic visit. No treatment regimen was given as a result of the adverse events. Patient had not been diagnosed with COVID-19 prior to vaccination and had not been tested since the vaccination. The outcome of event was recovering. No Follow-up attempts are possible. No further information is expected.

Other Meds: ACCUTANE

Current Illness:

ID: 1692733
Sex: F
Age:
State: PA

Vax Date: 03/13/2021
Onset Date: 04/16/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: A zone of papules and pruritis suggestive of shingles; A zone of papules and pruritis suggestive of shingles; A zone of papules and pruritis suggestive of shingles; This is a spontaneous report from a contactable Other HCP. A 72-years-old non pregnant female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EN6208), via an unspecified route of administration on 13Mar2021 at 10:00 am (at the age of 72-years-old) into Arm Left as a single dose for COVID-19 immunization at clinic. The patient had received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EL9266), via an unspecified route of administration on 20Feb2021 at 10:00 am into left arm as a single dose for COVID-19 immunization at clinic. Medical history included rheumatoid arthritis from an unknown date and unknown if ongoing Verbatim. The patient's concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The patient had no allergies. On 16Apr2021, the patient experienced A zone of papules and pruritis suggestive of shingles. No treatment was given for the events. The outcome of the events was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1692734
Sex: F
Age:
State:

Vax Date: 04/10/2021
Onset Date: 04/11/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Back pain, Cold sweat, Headache, Nausea, Vomiting

Symptoms: Headache- day 9th; fever; chills; diarrhea; nausea; muscle and joint pain; muscle and joint pain; injection site pain; exhaustion; feeling unwell; rash on my neck; This is a spontaneous report from a non-contactable consumer (patient) reported herself. A 43-years-old non-pregnant female patient received second dose of BNT162B2 (Pfizer-Biontech COVID-19 Vaccine, Solution for injection, lot number: ER 8829), via an unknown route of administration in left arm on 10Apr2021 (at the age of 43-years-old) as dose 2, single for Covid-19 immunisation at hospital. The patient's medical history included seasonal allergies and hazelnuts allergy. Concomitant medications included cetirizine hydrochloride [ZYRTEC (CETIRIZINE HYDROCHLORIDE)], bupropion (BUPROPION), phentermine (PHENTERMINE); were taken for an unknown indication from an unknown date. The patient previously received first dose of BNT162B2 as historical vaccine (Pfizer-Biontech COVID-19 Vaccine, Solution for injection, lot number: ER 8727), via an unknown route of administration in left arm on 20Mar2021 at 08:00 (at the age of 43-years-old) as dose 1, single for Covid-19 immunisation. No other vaccine in four weeks. On 11Apr2021 at 01:00, the patient experienced headache- day 9th (For first 3 days, headache), fever, chills, diarrhea, nausea, muscle and joint pain, injection site pain, exhaustion, feeling unwell, rash on my neck. Event resulted in visit to doctor or other healthcare professional office/clinic. No covid prior vaccination. No covid tested post vaccination. Migraine pills received as treatment. The outcome of the events was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: ZYRTEC [CETIRIZINE HYDROCHLORIDE]; BUPROPION; PHENTERMINE

Current Illness:

ID: 1692735
Sex: F
Age:
State: NV

Vax Date: 01/26/2021
Onset Date: 02/06/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025j20-2A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: Shingles; This is a spontaneous report from a contactable consumer (patient). A 72-year-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: FL1283, and Expiration date: Unknown), via an unspecified route of administration, administered in right arm on 26Jan2021 (at the age of 72-year-old) as dose 1, single for COVID-19 immunization. The patient medical history included allergies (known allergies). Concomitant medication included levothyroxine (LEVOTHYROXINE). The patient received unspecified other vaccine in four weeks. The patient did not have COVID prior to vaccination. The patient was not tested for COVID post vaccination. On 06Feb2021, the patient experienced shingles. The event resulted in Doctor or other healthcare professional office/clinic visit. No treatment was received for the event. The outcome of the event was reported as resolved on an unspecified date in 2021. No Follow-up attempts are possible. No Further information is expected.

Other Meds: LEVOTHYROXINE

Current Illness:

ID: 1692736
Sex: M
Age:
State: NY

Vax Date: 04/11/2021
Onset Date: 04/11/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data: Test Date: 20210412; Test Name: body temperature; Result Unstructured Data: Test Result:99

Allergies:

Symptom List: Chills, Diarrhoea, Fatigue, Feeling abnormal, Headache

Symptoms: Low grade fever (99); very tired; Chills; muscle pain; Joint pain; headache; Sore arm; Injection site pain; This is a spontaneous report from a non-contactable consumer, the patient. A 61-year-old male patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the right arm on 11Apr2021 at 16:00 (at the age of 61-year-old) as a single dose for COVID-19 immunisation. The patient had not reported any other health issue. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications included vitamin D (MANUFACTURER UNKNOWN) and nigella sativa seed oil (black cumin seed oil) (MANUFACTURER UNKNOWN) all from unknown date for unknown indication. The patient previously took Aspirin and experienced allergy to it. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the right arm on 21Mar2021 at 16:00 (at the age of 61-year-old) as a single dose for COVID-19 immunisation. On 11Apr2021, within a few minutes, the patient experienced injection site pain. On 12Apr2021 at 09:00, the patient experienced low grade fever (99) after 18 hours, tired, chills, muscle pain by 24 hours, joint pain, headache by 27 hours, very tired, and sore arm. Therapeutic measures were not taken for the events. The adverse event did not result in a visit to the doctors or other healthcare professional office/clinic visit, and emergency room/department or urgent. On 12Apr2021, the patient underwent body temperature and the result was 99 (unspecified units). The clinical outcome of the event injection site pain, low grade fever (99), chills, muscle pain was resolved in Apr2021, joint pain and headache was resolved on 13Apr2021, very tired was resolved on 14Apr2021 and sore arm was resolved on 15Apr2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds: VITAMIN D NOS; NIGELLA SATIVA SEED OIL

Current Illness:

ID: 1692737
Sex: M
Age:
State: NJ

Vax Date: 04/11/2021
Onset Date: 04/12/2021
Rec V Date: 09/11/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Hot flush, Myalgia, Nausea, Tension headache

Symptoms: Developed Shingles ( Zoster Herpes) within 24 hours of vaccine on same side and close to location of shot.; This is a spontaneous report from a contactable consumer or other non-health care professional (patient). A 62-years-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VAC-CINE, Formulation: Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration (at the age of 62-years), administered in left arm on 11Apr2021 at 16:30 as dose 1, single for COVID-19 immunization. Medical history included covid-19 from an unknown date and un-known if ongoing. Concomitant medications included krill oil (KRILL OIL) and probiotics (PROBIOTICS) taken for an unspecified indication, start and stop date were not reported. The patient did not receive any other vaccine in four weeks. The patient had covid prior vaccination and had not been tested for covid post vaccination. The patient had no known allergies. On 12Apr2021 at 20:00, the patient experi-enced developed shingles (zoster herpes) within 24 hours of vaccine on same side and close to loca-tion of shot. The treatment was received for the adverse event with valaciclovir. The adverse event resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. The clinical outcome for the events was reported as not recovered. No follow up attempts are possible; information about lot/batch cannot be obtained. No further information is expected.

Other Meds: KRILL OIL; PROBIOTICS

Current Illness:

Total 2021 VAERS Injuries: 654,986

Page last modified: 13 November 2021 9:17am